DoublecheQ Pregnancy Test 100-13

GUDID 00680243766491

The DoublecheQ Pregnancy Test is designed to be used for a qualitative determination of elevated human chorionic gonadotropin in urine. The result can be read visually in minutes to indicate a positive or negative result for pregnancy.

UNIVERSAL MEDITECH INC.

Total human chorionic gonadotropin (HCG) IVD, kit, immunochromatographic test (ICT), rapid

• Primary Device ID: 00680243766491
• NIH Device Record Key: 0f38e7c8-f976-4e02-b3e0-4adfdc7b8024
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DoublecheQ Pregnancy Test
• Version Model Number: Cassette
• Catalog Number: 100-13
• Company DUNS: 080243910
• Company Name: UNIVERSAL MEDITECH INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Operating and Storage Conditions

• Storage Environment Temperature: Between 36 Degrees Fahrenheit and 86 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00680243766491 [Primary]

FDA Product Code

• LCX: Kit, Test, Pregnancy, Hcg, Over The Counter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-06-28
• Device Publish Date: 2019-06-03

On-Brand Devices [DoublecheQ Pregnancy Test]

• 00680243766491: The DoublecheQ Pregnancy Test is designed to be used for a qualitative determination of elevated
• 00860002273006: The DoublecheQ Pregnancy Test is designed to be used for a qualitative determination of elevated